Identification of the principal catalytically important acidic residue of 3-hydroxy-3-methylglutaryl coenzyme A reductase.
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference33 articles.
1. Chemistry, biochemistry, and pharmacology of HMG-CoA reductase inhibitors
2. Pyridine nucleotide-linked four-electron transfer dehydrogenases
3. Pseudomonas mevalonii 3-hydroxy-3-methylglutaryl-CoA reductase
4. Kinetic analysis of the individual reductive steps catalyzed by β-hydroxy-β-methylglutaryl-coenzyme A reductase obtained from yeast
5. Rat liver 3-hydroxy-3-methylglutaryl-CoA reductase. Catalysis of the reverse reaction and two half-reactions.
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2. Point mutations in Candida glabrata 3-hydroxy-3-methylglutaryl-coenzyme A reductase (CgHMGR) decrease enzymatic activity and substrate/inhibitor affinity;Scientific Reports;2021-10-21
3. Latex proteins and enzymes involved in terpenoid biosynthesis of selected Euphorbia species: Euphorbia kansui Liou and Euphorbia helioscopia L.;Advances in Botanical Research;2020
4. cDNA cloning, prokaryotic expression and functional analysis of 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGCR) in Pogostemon cablin;Protein Expression and Purification;2019-11
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